McEnery M W
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Bioenerg Biomembr. 1992 Feb;24(1):63-9. doi: 10.1007/BF00769532.
Specific, high-affinity receptors for numerous drugs have recently been localized to mitochondrial membrane proteins. This review discusses the association of the mitochondrial receptor for benzodiazepines (mBzR) with the voltage-dependent anion channel (VDAC), indicating a possible auxiliary role for VDAC as a putative drug binding protein. The proposed subunit composition of the purified mBzR complex isolated from rat kidney mitochondria includes VDAC, which functions as a recognition site for benzodiazepines (e.g., flunitrazepam), the adenine nucleotide carrier (ADC), and an 18 kDa outer membrane protein identified by covalent labelling with the mBzR antagonists isoquinoline carboxamides (e.g., PK14105).
最近,已将许多药物的特异性、高亲和力受体定位到线粒体膜蛋白上。本综述讨论了苯二氮䓬类药物的线粒体受体(mBzR)与电压依赖性阴离子通道(VDAC)的关联,表明VDAC作为一种假定的药物结合蛋白可能具有辅助作用。从大鼠肾线粒体中分离出的纯化mBzR复合物的拟议亚基组成包括VDAC,其作为苯二氮䓬类药物(如氟硝西泮)的识别位点发挥作用、腺嘌呤核苷酸载体(ADC),以及通过与mBzR拮抗剂异喹啉羧酰胺(如PK14105)进行共价标记鉴定出的一种18 kDa外膜蛋白。